The 20 Best Mitochondrial Trifunctional Protein Deficiency Doctors Near Me
Find the Top Mitochondrial Trifunctional Protein Deficiency Experts and Specialists
OSF Illinois Neurological Institute - Neurology
Gregory Blume is a Neurologist practicing medicine in Peoria, Illinois. Dr. Blume is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Paramyotonia Congenita, Myotonic Dystrophy Type 2, and Myotonic Dystrophy. Dr. Blume is board certified in American Board Of Psychiatry And Neurology.
Vanderbilt Medical Group- Teleneurology
Christopher Lee is a Neurologist practicing medicine in Nashville, Tennessee. Dr. Lee is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 32 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Spinal Muscular Atrophy (SMA), Guillain-Barre Syndrome, and Gamma Knife Radiosurgery. Dr. Lee is board certified in American Board Of Psychiatry & Neurology.
Office
Eroboghene Ubogu is a Neurologist practicing medicine in Birmingham, Alabama. Dr. Ubogu is rated as a Distinguished provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 59 other conditions, according to our data. His clinical expertise encompasses Chronic Inflammatory Demyelinating Polyneuropathy, Guillain-Barre Syndrome, Mitochondrial Complex 2 Deficiency, and Mitochondrial Complex 3 Deficiency.
St. Christopher's Pediatric Associates Genetics - E. Erie Avenue
Georgianne Arnold is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Arnold is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Mitochondrial Trifunctional Protein Deficiency, Krabbe Disease, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. Arnold is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.
University Of Texas Southwestern Medical Center At Dallas
Maryjane Farr is an Advanced Heart Failure and Transplant Cardiologist and a Cardiologist practicing medicine in Dallas, Texas. Dr. Farr is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Heart Failure, Cardiogenic Shock, Cardiomyopathy, Pulmonary Edema, and Heart Transplant.
OSF Illinois Neurological Institute
Brandon Strawn is a Neurologist practicing medicine in Rockford, Illinois. Dr. Strawn is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. His clinical expertise encompasses Memory Loss, Headache, Cerebellar Degeneration, and Peripheral Neuropathy. Dr. Strawn is board certified in American Board Of Psychiatry And Neurology.
Texas Health Family Care
John Hoffman is a primary care provider, practicing in Family Medicine in Burleson, Texas. Dr. Hoffman is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses High Cholesterol, Familial Combined Hyperlipidemia, Xanthoma, and Glucocorticoid-Remediable Aldosteronism.
Lenox Baker Children's Hospital
I find joy and satisfaction in my dedication to the care of children with rare diseases specifically: genetic disorders and inherited disorders of metabolism. Due to many years of training and practice, I have experience involving care of patients with a variety of genetic and metabolic conditions, including but not limited to glycogen storage diseases, fatty acid oxidation defects, mitochondrial disorders, lysosomal storage diseases, urea cycle disorders, organic acidurias, aminoacidopathies, and infantile hepatopathy due to LARS mutations, etc. I enjoy working together with children and their parents, whom I consider an important part of the team. I pursued this field because it gives me great satisfaction and pleasure to see the children with these conditions grow, and the patients and families feel cared for, and not isolated. I love learning about the children's interests, and see that they grow happy and healthy. I think out of the box when there is a challenge that needs to be met for the patient's care and management. Dr. Hassan is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Mitochondrial Trifunctional Protein Deficiency, Protein Deficiency, Von Gierke Disease, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. Hassan is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics and American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics.
Cesar D. Hadalgo, MD
Cesar Hidalgo is a Neurologist and a Neuromusculoskeletal Medicine provider practicing medicine in Rochester Hills, Michigan. He has been practicing medicine for over 52 years. Dr. Hidalgo is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Multiple Sclerosis (MS), Transient Ischemic Attack (TIA), Myasthenia Gravis, and Coenzyme Q Cytochrome C Reductase Deficiency. Dr. Hidalgo is board certified in American Board Of Psychiatry And Neurology, American Board Of Psychiatry And Neurology, American Board Of Psychiatry And Neurology, and American Board Of Psychiatry And Neurology. Dr. Hidalgo is currently accepting new patients.
Duke Electromyography Laboratory - Clinic 1L
Vern Juel is a Neurologist practicing medicine in Durham, North Carolina. He has been practicing medicine for over 37 years. Dr. Juel is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 71 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Lambert-Eaton Syndrome, Inclusion Body Myositis, Meige Syndrome, and Thymectomy. Dr. Juel is board certified in American Board Of Psychiatry/Neurology, Clinical Neurophysiology , American Board Of Psychiatry/Neurology, Neurology , and American Board Of Psychiatry/Neurology, Neuromuscular Medicine.
UPMC Vision Institute
Jose' Sahel is an Ophthalmologist practicing medicine in Pittsburgh, Pennsylvania. Dr. Sahel is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 35 other conditions, according to our data. His clinical expertise encompasses Retinopathy Pigmentary Mental Retardation, Cone-Rod Dystrophy, X-Linked Congenital Stationary Night Blindness, Retinitis Pigmentosa, and Vitrectomy. Dr. Sahel is currently accepting new patients.
Duke Electromyography Laboratory - Clinic 1L
I care for patients with neuromuscular disorders, which include muscular dystrophy, neuropathy, autoimmune muscle, and nerve conditions, as well as inherited ones. A lot of my work is focused on a holistic approach, so I don’t just focus on the treatment of the disease, but also the way the disease is affecting the rest of the patient’s life and quality of life. I will spend the majority of my visit talking with the patient, then do a full neurological exam, and then discuss potential options and potential diagnoses. If it is a condition that is autoimmune, we can discuss various therapies that can be used and other needs at home related to mobility or basic function. Our patients have a variety of different conditions that can cause problems with breathing, cardiac abnormalities, endocrine dysfunction, and mobility problems. Our clinic here at Duke is unique because we offer multiple consultants working as a team to give the best holistic care to a patient. Dr. Raja is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Myasthenia Gravis, Lambert-Eaton Syndrome, Coenzyme Q Cytochrome C Reductase Deficiency, Mitochondrial Complex 1 Deficiency, and Thymectomy. Dr. Raja is board certified in American Board Of Psychiatry/Neurology, Neurology and American Board Of Psychiatry/Neurology, Neuromuscular Medicine.
Kennedy Krieger Institute
Dr. Leung obtained her undergraduate degree in biochemical sciences from Harvard University. While attending medical school at Duke University, she completed a year-long research fellowship studying genetic markers of late-onset Alzheimer’s disease at the National Institute on Aging as part of the NIH Clinical Research Training Program. She completed her neurology residency and clinical neurophysiology fellowship at Stanford University Medical Center, and is currently a Ph.D. candidate in the graduate training program in clinical investigation at the Johns Hopkins Bloomberg School of Public Health. Dr. Leung joined the Center for Genetic Muscle Disorders at the Kennedy Krieger Institute as a translational research fellow in 2010 and was appointed to the faculty in 2014. Her clinic specializes in electromyography and the diagnosis and treatment of hereditary muscle diseases. Dr. Leung’s research focuses on the development of imaging biomarkers and outcome measures for muscle diseases. She is the principal investigator for a longitudinal cohort study of whole-body MRI in facioscapulohumeral muscular dystrophy. Dr. Leung is also a site principal investigator for the Ionis-DMPKRx trial, a phase Ib/IIa clinical trial of a novel RNA-based therapy for myotonic muscular dystrophy. Dr. Leung is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Facioscapulohumeral Muscular Dystrophy (FSHD), Limb-Girdle Muscular Dystrophy Type 2I, Limb-Girdle Muscular Dystrophy, and Dysferlinopathy. Dr. Leung is board certified in American Board Of Psychiatry And Neurology.
Neurological Sciences Center At Clarkson Doctors Building North
Pariwat Thaisetthawatkul is a Neurologist practicing medicine in Omaha, Nebraska. He has been practicing medicine for over 36 years. Dr. Thaisetthawatkul is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 45 other conditions, according to our data. His clinical expertise encompasses Stiff Person Syndrome, Chronic Inflammatory Demyelinating Polyneuropathy, Myasthenia Gravis, and Inclusion Body Myositis.
Duke University Hospital
My practice includes caring for children and adults with inherited conditions, such as inherited disorders of metabolism, genetic syndromes, mitochondrial disorders, inherited causes of growth failure or developmental delay, and conditions detected by newborn screening. My clinic works with the Pediatric Biochemical Genetics Laboratory to diagnose these conditions. We provide treatment for inherited disorders of metabolism. I work closely with the geneticists, neurologists, pediatricians, internists, and other providers at Duke University Medical Center to provide comprehensive care for my patients. My research has been aimed at developing new treatments for inherited conditions, focusing on glycogen storage diseases, like Pompe disease and von Gierke disease. We have developed gene therapy for these conditions and are in the process of starting clinical trials to test safety and benefits. Dr. Koeberl is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Von Gierke Disease, X-Linked Creatine Deficiency, and Kearns-Sayre Syndrome. Dr. Koeberl is board certified in American Board Of Medical Genetics, Clinical Biochemical Genetics , American Board Of Medical Genetics, Clinical Genetics And Genomics - General , and American Board Of Pediatrics, General Pediatrics.
Penn Heart And Vascular Center
Anjali Owens is a Cardiologist practicing medicine in Philadelphia, Pennsylvania. Dr. Owens is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Cardiomyopathy, Hypertrophic Cardiomyopathy (HCM), Familial Hypertrophic Cardiomyopathy, Dilated Cardiomyopathy (DCM), and Heart Transplant. Dr. Owens is currently accepting new patients.
Corewell Health Grand Rapids Hospitals Neurology - 2750 E Beltline Ave NE
Paul Twydell is a Neuromusculoskeletal Medicine specialist and a Neurologist practicing medicine in Grand Rapids, Michigan. He has been practicing medicine for over 26 years. Dr. Twydell is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 31 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Monomelic Amyotrophy, Chronic Inflammatory Demyelinating Polyneuropathy, and Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease). Dr. Twydell is board certified in American Board Of Psychiatry And Neurology. Dr. Twydell is currently accepting new patients.
Duke Electromyography Laboratory - Clinic 1L
I have dedicated my professional life to treating patients with neuromuscular disorders. These include neuropathy (GBS, CIDP), myopathy, Myasthenia Gravis, and ALS. I incorporate the use of electromyography (EMG), whenever appropriate, to help diagnosis my patients and start proper therapy. My greatest satisfaction as a doctor is helping patients improve and forming lasting relationships. I want my patients to feel like they are not alone navigating their disease and know I will be there for them every step of the way. Duke Health is truly a world-class institution. Dr. Mayberry is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Stiff Person Syndrome, Coenzyme Q Cytochrome C Reductase Deficiency, Mitochondrial Complex 1 Deficiency, and Mitochondrial Trifunctional Protein Deficiency. Dr. Mayberry is board certified in American Board Of Psychiatry/Neurology, Neurology and American Board Of Psychiatry/Neurology, Neuromuscular Medicine.
Cleveland Clinic Main Campus
Sumit Parikh is a Pediatric Neurologist practicing medicine in Cleveland, Ohio. He has been practicing medicine for over 32 years. Dr. Parikh is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. He is also highly rated in 168 other conditions, according to our data. His clinical expertise encompasses Kearns-Sayre Syndrome, Maternally Inherited Leigh Syndrome, Leigh Syndrome, and MELAS Syndrome. Dr. Parikh is board certified in American Board Of Psychiatry And Neurology, 2006.
Rubenstein Child Health Building
Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, and Progressive External Ophthalmoplegia. Dr. Vernon is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.
Last Updated: 04/28/2026
















